JP2011503233A5 - - Google Patents
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- Publication number
- JP2011503233A5 JP2011503233A5 JP2010535014A JP2010535014A JP2011503233A5 JP 2011503233 A5 JP2011503233 A5 JP 2011503233A5 JP 2010535014 A JP2010535014 A JP 2010535014A JP 2010535014 A JP2010535014 A JP 2010535014A JP 2011503233 A5 JP2011503233 A5 JP 2011503233A5
- Authority
- JP
- Japan
- Prior art keywords
- yloxy
- pyridin
- diazepan
- methanone
- tetrahydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 17
- 125000000217 alkyl group Chemical group 0.000 claims 15
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 15
- -1 cyclocyclobutyl Chemical group 0.000 claims 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 208000035475 disorder Diseases 0.000 claims 8
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 7
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 4
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 claims 4
- 206010041349 Somnolence Diseases 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 208000010877 cognitive disease Diseases 0.000 claims 4
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 3
- 208000032140 Sleepiness Diseases 0.000 claims 3
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 230000006735 deficit Effects 0.000 claims 3
- 206010027175 memory impairment Diseases 0.000 claims 3
- 239000002207 metabolite Substances 0.000 claims 3
- 239000000651 prodrug Substances 0.000 claims 3
- 229940002612 prodrug Drugs 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 208000019116 sleep disease Diseases 0.000 claims 3
- QVUOERZYMAHRRW-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 QVUOERZYMAHRRW-UHFFFAOYSA-N 0.000 claims 2
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 2
- 208000001573 Cataplexy Diseases 0.000 claims 2
- 208000028698 Cognitive impairment Diseases 0.000 claims 2
- 208000030814 Eating disease Diseases 0.000 claims 2
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 235000014632 disordered eating Nutrition 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 206010016256 fatigue Diseases 0.000 claims 2
- 229960001340 histamine Drugs 0.000 claims 2
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 102000005962 receptors Human genes 0.000 claims 2
- 108020003175 receptors Proteins 0.000 claims 2
- VXAJSHFQQHNGQX-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-(6-cyclobutyloxypyridin-3-yl)methanone Chemical compound C=1C=C(OC2CCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 VXAJSHFQQHNGQX-UHFFFAOYSA-N 0.000 claims 1
- YNZIFJAHDHVCJE-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-(6-cyclohexyloxypyridin-3-yl)methanone Chemical compound C=1C=C(OC2CCCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 YNZIFJAHDHVCJE-UHFFFAOYSA-N 0.000 claims 1
- ATMRCNUBMGDAJB-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-(6-cyclopentyloxypyridin-3-yl)methanone Chemical compound C=1C=C(OC2CCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 ATMRCNUBMGDAJB-UHFFFAOYSA-N 0.000 claims 1
- JTJVOKQSNSXDSQ-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[5-(oxan-4-yloxy)pyridin-2-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)C=NC=1C(=O)N(CC1)CCCN1C1CCC1 JTJVOKQSNSXDSQ-UHFFFAOYSA-N 0.000 claims 1
- WERIDDXCKXMLPN-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(1-ethylazepan-3-yl)oxypyridin-3-yl]methanone Chemical compound C1N(CC)CCCCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 WERIDDXCKXMLPN-UHFFFAOYSA-N 0.000 claims 1
- UWCKCKPVQKWRLE-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(1-methylpiperidin-4-yl)oxypyridin-3-yl]methanone Chemical compound C1CN(C)CCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 UWCKCKPVQKWRLE-UHFFFAOYSA-N 0.000 claims 1
- QIIMXKWOAINTGQ-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(1-methylpyrrolidin-3-yl)oxypyridin-3-yl]methanone Chemical compound C1N(C)CCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 QIIMXKWOAINTGQ-UHFFFAOYSA-N 0.000 claims 1
- CIZGYGDRXHSNNY-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(1-propan-2-ylazepan-4-yl)oxypyridin-3-yl]methanone Chemical compound C1CN(C(C)C)CCCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 CIZGYGDRXHSNNY-UHFFFAOYSA-N 0.000 claims 1
- OBURCTXWJHSPOX-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(cyclobutylmethoxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OCC2CCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 OBURCTXWJHSPOX-UHFFFAOYSA-N 0.000 claims 1
- VEXRDBRLGWUOJS-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(cyclopropylmethoxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OCC2CC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 VEXRDBRLGWUOJS-UHFFFAOYSA-N 0.000 claims 1
- OXXUXAYRUZNWAN-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(oxan-4-yloxy)pyridin-2-yl]methanone Chemical compound C=1C=CC(OC2CCOCC2)=NC=1C(=O)N(CC1)CCCN1C1CCC1 OXXUXAYRUZNWAN-UHFFFAOYSA-N 0.000 claims 1
- NUYACTQCGLVCMC-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(oxepan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2COCCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 NUYACTQCGLVCMC-UHFFFAOYSA-N 0.000 claims 1
- LRPQZEPPDZMKDA-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(oxepan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 LRPQZEPPDZMKDA-UHFFFAOYSA-N 0.000 claims 1
- BFJLVORPAXGFKY-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(oxolan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2COCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 BFJLVORPAXGFKY-UHFFFAOYSA-N 0.000 claims 1
- YWTLQMXBLFRANM-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(thian-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCSCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 YWTLQMXBLFRANM-UHFFFAOYSA-N 0.000 claims 1
- CPBJQSTWGOQQPN-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(thiepan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CSCCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 CPBJQSTWGOQQPN-UHFFFAOYSA-N 0.000 claims 1
- XAEOEVMPYKYFCO-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(thiepan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCSCCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 XAEOEVMPYKYFCO-UHFFFAOYSA-N 0.000 claims 1
- IDOPSVITNKOECG-UHFFFAOYSA-N (4-cyclobutyl-1,4-diazepan-1-yl)-[6-(thiolan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CSCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCC1 IDOPSVITNKOECG-UHFFFAOYSA-N 0.000 claims 1
- MGCIMRQKRGCWIW-UHFFFAOYSA-N (4-cyclobutylpiperazin-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCN1C1CCC1 MGCIMRQKRGCWIW-UHFFFAOYSA-N 0.000 claims 1
- ZAMBPCHSYIEQEW-UHFFFAOYSA-N (4-cyclopentyl-1,4-diazepan-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCCN1C1CCCC1 ZAMBPCHSYIEQEW-UHFFFAOYSA-N 0.000 claims 1
- HIJUMTVHMNNALA-UHFFFAOYSA-N (4-cyclopentylpiperazin-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCN1C1CCCC1 HIJUMTVHMNNALA-UHFFFAOYSA-N 0.000 claims 1
- GDEYUSKKFOOEFV-UHFFFAOYSA-N (4-cyclopropyl-1,4-diazepan-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCCN1C1CC1 GDEYUSKKFOOEFV-UHFFFAOYSA-N 0.000 claims 1
- VRDXIGWWUIWIRM-UHFFFAOYSA-N (4-cyclopropyl-1,4-diazepan-1-yl)-[6-(oxolan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2COCC2)N=CC=1C(=O)N(CC1)CCCN1C1CC1 VRDXIGWWUIWIRM-UHFFFAOYSA-N 0.000 claims 1
- LBRUZEHUUYGSJN-UHFFFAOYSA-N (4-cyclopropylpiperazin-1-yl)-[6-(oxan-3-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2COCCC2)N=CC=1C(=O)N(CC1)CCN1C1CC1 LBRUZEHUUYGSJN-UHFFFAOYSA-N 0.000 claims 1
- XOUOBAGFBFSLMB-UHFFFAOYSA-N (4-cyclopropylpiperazin-1-yl)-[6-(oxan-4-yloxy)pyridin-3-yl]methanone Chemical compound C=1C=C(OC2CCOCC2)N=CC=1C(=O)N(CC1)CCN1C1CC1 XOUOBAGFBFSLMB-UHFFFAOYSA-N 0.000 claims 1
- GQSAFMNDDDSCJD-UHFFFAOYSA-N 1-[3-[5-(4-cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yl]oxypyrrolidin-1-yl]ethanone Chemical compound C1N(C(=O)C)CCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 GQSAFMNDDDSCJD-UHFFFAOYSA-N 0.000 claims 1
- CYUFBNIXXRIJMO-UHFFFAOYSA-N 1-[4-[5-(4-cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yl]oxyazepan-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 CYUFBNIXXRIJMO-UHFFFAOYSA-N 0.000 claims 1
- WRMDPNFCGVUCEJ-UHFFFAOYSA-N 1-[4-[5-(4-cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yl]oxypiperidin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCC1OC1=CC=C(C(=O)N2CCN(CCC2)C2CCC2)C=N1 WRMDPNFCGVUCEJ-UHFFFAOYSA-N 0.000 claims 1
- ZWEWUVQWWYKCEY-UHFFFAOYSA-N 3-cyclohexyloxy-6-(4-cyclopropyl-1,4-diazepane-1-carbonyl)pyridine-2-carbonitrile Chemical compound C=1C=C(OC2CCCCC2)C(C#N)=NC=1C(=O)N(CC1)CCCN1C1CC1 ZWEWUVQWWYKCEY-UHFFFAOYSA-N 0.000 claims 1
- HWIBZEXREFGUOK-UHFFFAOYSA-N 3-cyclopentyloxy-6-(4-cyclopropyl-1,4-diazepane-1-carbonyl)pyridine-2-carbonitrile Chemical compound C=1C=C(OC2CCCC2)C(C#N)=NC=1C(=O)N(CC1)CCCN1C1CC1 HWIBZEXREFGUOK-UHFFFAOYSA-N 0.000 claims 1
- NVXAPLQKZORNMX-UHFFFAOYSA-N 6-(4-cyclopropyl-1,4-diazepane-1-carbonyl)-3-(oxolan-3-yloxy)pyridine-2-carbonitrile Chemical compound C=1C=C(OC2COCC2)C(C#N)=NC=1C(=O)N(CC1)CCCN1C1CC1 NVXAPLQKZORNMX-UHFFFAOYSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- 208000017164 Chronobiology disease Diseases 0.000 claims 1
- 208000019888 Circadian rhythm sleep disease Diseases 0.000 claims 1
- 206010010904 Convulsion Diseases 0.000 claims 1
- 206010012289 Dementia Diseases 0.000 claims 1
- 208000007590 Disorders of Excessive Somnolence Diseases 0.000 claims 1
- 201000010374 Down Syndrome Diseases 0.000 claims 1
- 208000001456 Jet Lag Syndrome Diseases 0.000 claims 1
- 208000020358 Learning disease Diseases 0.000 claims 1
- 206010026749 Mania Diseases 0.000 claims 1
- 208000026139 Memory disease Diseases 0.000 claims 1
- 208000019695 Migraine disease Diseases 0.000 claims 1
- 208000016285 Movement disease Diseases 0.000 claims 1
- 208000007920 Neurogenic Inflammation Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000005793 Restless legs syndrome Diseases 0.000 claims 1
- 208000007014 Retinitis pigmentosa Diseases 0.000 claims 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 claims 1
- 208000009205 Tinnitus Diseases 0.000 claims 1
- YTYZYBQMJSYXCS-UHFFFAOYSA-N [6-(oxan-4-yloxy)pyridin-3-yl]-(4-propan-2-yl-1,4-diazepan-1-yl)methanone Chemical compound C1CN(C(C)C)CCCN1C(=O)C(C=N1)=CC=C1OC1CCOCC1 YTYZYBQMJSYXCS-UHFFFAOYSA-N 0.000 claims 1
- QVCDNGPZHDYLTF-UHFFFAOYSA-N [6-(oxan-4-yloxy)pyridin-3-yl]-(4-propan-2-ylpiperazin-1-yl)methanone Chemical compound C1CN(C(C)C)CCN1C(=O)C(C=N1)=CC=C1OC1CCOCC1 QVCDNGPZHDYLTF-UHFFFAOYSA-N 0.000 claims 1
- AOAATJGNDYOJLI-UHFFFAOYSA-N [6-(oxolan-3-yloxy)pyridin-3-yl]-(4-propan-2-yl-1,4-diazepan-1-yl)methanone Chemical compound C1CN(C(C)C)CCCN1C(=O)C(C=N1)=CC=C1OC1COCC1 AOAATJGNDYOJLI-UHFFFAOYSA-N 0.000 claims 1
- QFMMEHWYAXVVKG-UHFFFAOYSA-N [6-(oxolan-3-yloxy)pyridin-3-yl]-(4-propan-2-ylpiperazin-1-yl)methanone Chemical compound C1CN(C(C)C)CCN1C(=O)C(C=N1)=CC=C1OC1COCC1 QFMMEHWYAXVVKG-UHFFFAOYSA-N 0.000 claims 1
- JOQCUMLLZBXYRU-UHFFFAOYSA-N [6-[(3-methyloxetan-3-yl)methoxy]pyridin-3-yl]-(4-propan-2-yl-1,4-diazepan-1-yl)methanone Chemical compound C1CN(C(C)C)CCCN1C(=O)C(C=N1)=CC=C1OCC1(C)COC1 JOQCUMLLZBXYRU-UHFFFAOYSA-N 0.000 claims 1
- PSQBHHXUGLRPQZ-UHFFFAOYSA-N [6-[(3-methyloxetan-3-yl)methoxy]pyridin-3-yl]-(4-propan-2-ylpiperazin-1-yl)methanone Chemical compound C1CN(C(C)C)CCN1C(=O)C(C=N1)=CC=C1OCC1(C)COC1 PSQBHHXUGLRPQZ-UHFFFAOYSA-N 0.000 claims 1
- 230000007000 age related cognitive decline Effects 0.000 claims 1
- 125000003725 azepanyl group Chemical group 0.000 claims 1
- 238000002512 chemotherapy Methods 0.000 claims 1
- 230000002920 convulsive effect Effects 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 208000002173 dizziness Diseases 0.000 claims 1
- 206010015037 epilepsy Diseases 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000013632 homeostatic process Effects 0.000 claims 1
- 230000003054 hormonal effect Effects 0.000 claims 1
- 206010022437 insomnia Diseases 0.000 claims 1
- 208000033915 jet lag type circadian rhythm sleep disease Diseases 0.000 claims 1
- 201000003723 learning disability Diseases 0.000 claims 1
- 208000002780 macular degeneration Diseases 0.000 claims 1
- 230000009245 menopause Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 206010027599 migraine Diseases 0.000 claims 1
- 208000027061 mild cognitive impairment Diseases 0.000 claims 1
- 201000003152 motion sickness Diseases 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- 201000003631 narcolepsy Diseases 0.000 claims 1
- 208000004296 neuralgia Diseases 0.000 claims 1
- 208000021722 neuropathic pain Diseases 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 125000003551 oxepanyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 208000028173 post-traumatic stress disease Diseases 0.000 claims 1
- 208000020016 psychiatric disease Diseases 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 201000002859 sleep apnea Diseases 0.000 claims 1
- 201000009032 substance abuse Diseases 0.000 claims 1
- 231100000736 substance abuse Toxicity 0.000 claims 1
- 208000011117 substance-related disease Diseases 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000001583 thiepanyl group Chemical group 0.000 claims 1
- 231100000886 tinnitus Toxicity 0.000 claims 1
- 0 C*1(CCN(*)CC1)C(C1=CC=C(*)**1)=O Chemical compound C*1(CCN(*)CC1)C(C1=CC=C(*)**1)=O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98924607P | 2007-11-20 | 2007-11-20 | |
| US60/989,246 | 2007-11-20 | ||
| PCT/US2008/083764 WO2009067401A1 (en) | 2007-11-20 | 2008-11-17 | Cycloalkyloxy-and hetξrocycloalky- loxypyridine compounds as modulators of the histamine h3 receptor |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011503233A JP2011503233A (ja) | 2011-01-27 |
| JP2011503233A5 true JP2011503233A5 (enExample) | 2012-01-05 |
| JP5498390B2 JP5498390B2 (ja) | 2014-05-21 |
Family
ID=40297867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010535014A Expired - Fee Related JP5498390B2 (ja) | 2007-11-20 | 2008-11-17 | ヒスタミンｈ３受容体のモジュレーターとしてのシクロアルキルオキシ−及びヘテロシクロアルキルオキシピリジン化合物 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8883776B2 (enExample) |
| EP (1) | EP2222664B1 (enExample) |
| JP (1) | JP5498390B2 (enExample) |
| KR (1) | KR101546712B1 (enExample) |
| CN (2) | CN105712977B (enExample) |
| AR (2) | AR069387A1 (enExample) |
| AU (1) | AU2008326561B2 (enExample) |
| BR (1) | BRPI0820481A2 (enExample) |
| CA (1) | CA2706328C (enExample) |
| CL (1) | CL2008003465A1 (enExample) |
| CO (1) | CO6210700A2 (enExample) |
| CR (1) | CR11529A (enExample) |
| EA (1) | EA018582B1 (enExample) |
| EC (1) | ECSP10010190A (enExample) |
| MX (1) | MX2010005488A (enExample) |
| MY (1) | MY158253A (enExample) |
| NI (1) | NI201000086A (enExample) |
| NZ (1) | NZ584998A (enExample) |
| TW (1) | TWI491604B (enExample) |
| UA (1) | UA103468C2 (enExample) |
| WO (1) | WO2009067401A1 (enExample) |
| ZA (1) | ZA201004334B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0324159D0 (en) | 2003-10-15 | 2003-11-19 | Glaxo Group Ltd | Novel compounds |
| US20090170869A1 (en) * | 2007-09-06 | 2009-07-02 | Desmond John Best | Piperazine derivative having affinity for the histamine h3 receptor |
| US20090318380A1 (en) | 2007-11-20 | 2009-12-24 | Pharmasset, Inc. | 2',4'-substituted nucleosides as antiviral agents |
| CA2721303C (en) * | 2008-05-08 | 2016-06-28 | Evotec Ag | Azetidines and cyclobutanes as histamine h3 receptor antagonists |
| AU2010226711B2 (en) * | 2009-03-18 | 2015-06-18 | Janssen Pharmaceutica Nv | Process for the preparation of histamine H3 receptor modulators |
| MX2012003394A (es) * | 2009-09-21 | 2012-08-15 | Univ Vanderbilt | Analogos de la nicotinamida de o-bencilo como moduladores alostéricos positivos del mglur5. |
| SI2729130T1 (en) | 2011-07-07 | 2018-03-30 | Janssen Sciences Ireland Uc | Combined formulations of darunavir |
Family Cites Families (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE817911C (de) | 1947-12-16 | 1951-10-22 | Chem Fab Tempelhof Preuss & Te | Verfahren zur Darstellung von in 6-Stellung basisch substituierten Pyridin-3-carbonsaeureamiden |
| BE726551A (enExample) | 1968-01-22 | 1969-06-16 | ||
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- 2008-11-17 MX MX2010005488A patent/MX2010005488A/es active IP Right Grant
- 2008-11-17 US US12/272,268 patent/US8883776B2/en not_active Expired - Fee Related
- 2008-11-17 EA EA201070637A patent/EA018582B1/ru unknown
- 2008-11-17 CA CA2706328A patent/CA2706328C/en not_active Expired - Fee Related
- 2008-11-17 UA UAA201007603A patent/UA103468C2/ru unknown
- 2008-11-17 AU AU2008326561A patent/AU2008326561B2/en not_active Ceased
- 2008-11-17 MY MYPI2010002288A patent/MY158253A/en unknown
- 2008-11-17 CN CN201610094782.9A patent/CN105712977B/zh not_active Expired - Fee Related
- 2008-11-17 KR KR1020107013252A patent/KR101546712B1/ko not_active Expired - Fee Related
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- 2008-11-17 EP EP08852442.6A patent/EP2222664B1/en not_active Not-in-force
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